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Cellular processes associated with LRRK2 function and dysfunction
Mutations in the leucine‐rich repeat kinase 2 (LRRK2)‐encoding gene are the most common cause of monogenic Parkinson's disease. The identification of LRRK2 polymorphisms associated with increased risk for sporadic Parkinson's disease, as well as the observation that LRRK2‐Parkinson's...
Guardat en:
| Publicat a: | FEBS J |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley and Sons Inc.
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4522467/ https://ncbi.nlm.nih.gov/pubmed/25899482 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/febs.13305 |
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